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首页> 外文期刊>Journal of pharmaceutical sciences. >Determination of drug-polymer binding constants by affinity capillary electrophoresis for aryl propionic acid derivatives and related compounds
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Determination of drug-polymer binding constants by affinity capillary electrophoresis for aryl propionic acid derivatives and related compounds

机译:亲和毛细管电泳法测定芳基丙酸衍生物及相关化合物的药物-聚合物结合常数

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摘要

The binding constants (Kbs) of 17 aryl propionic acid derivatives (APADs) and related compounds with polyvinylpyrrolidone (PVP K30) and vinylpyrrolidone-vinyl acetate copolymer (Kollidon VA64) in aqueous media were determined by affinity capillary electrophoreses (ACE). The Kbs of APAD to polymers increase with octanol-water partition coefficients of the compounds. Kollidon VA64 is a stronger binder than PVP K30 to APAD compounds. The Kbs are greater at pH 4 than at pH 9. Both hydrophobic interaction and hydrogen bonding may be involved. However, hydrophobic interaction appears to be dominant. The ACE method is simple and fast, which could be used to study drug-polymer interaction in aqueous media.
机译:通过亲和毛细管电泳(ACE)测定了17种芳基丙酸衍生物(APADs)和相关化合物与聚乙烯吡咯烷酮(PVP K30)和乙烯基吡咯烷酮-乙酸乙烯酯共聚物(Kollidon VA64)的结合常数(Kbs)。 APAD对聚合物的Kbs随着化合物的辛醇-水分配系数而增加。与PAD K30相比,Kollidon VA64对APAD化合物具有更强的结合力。在pH 4时,Kb比在pH 9时大。疏水相互作用和氢键均可参与。但是,疏水相互作用似乎是主要的。 ACE方法简便,快速,可用于研究水性介质中的药物-聚合物相互作用。

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